17325-02-9

Basic information

• Product Name: (E)-3-Amino-3-(4-methoxy-phenyl)-acrylonitrile
• CAS NO: 17325-02-9
• Molecular Weight: 174.202
• Mol File: 17325-02-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (E)-3-Amino-3-(4-methoxy-phenyl)-acrylonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-Amino-3-(4-methoxy-phenyl)-acrylonitrile(17325-02-9)
• EPA Substance Registry System: (E)-3-Amino-3-(4-methoxy-phenyl)-acrylonitrile(17325-02-9)

Safety Data

• Hazardous Substances Data: 17325-02-9(Hazardous Substances Data)

Upstream product

• 874-90-8 4-methoxybenzonitrile 
• 75-05-8 acetonitrile 
• 104-47-2 p-methoxybenzylnitrile 

Downstream Products

• 128421-64-7 3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-(4-methoxy-phenyl)-isoxazole-4-carbonitrile 
• 128421-48-7 (Z)-2-[3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-[1,2,4]oxadiazol-5-yl]-1-(4-methoxy-phenyl)-vinylamine 
• 3672-47-7 3-oxo-3-(4'-methoxyphenyl)propanenitrile 
• 1233219-50-5 3-acetylamino-3-(p-methoxyphenyl)acrylonitrile 
• 97746-16-2 5,7-dihydroxy-4-(4-methoxyphenyl)-2H-1-benzopyran-2-one 
• 124413-47-4 3,5-dicyano-2,6-di-p-methoxyphenylpyridine 
• 124413-57-6 3-amino-2-(N-phenylformimidoyl)-4'-methoxyallocinnamonitrile 
• 124413-58-7 3-amino-2-(N-cyclohexylformimidoyl)-4'-methoxyallocinnamonitrile 
• 124413-44-1 4-cyano-3-(p-methoxyphenyl)isothiazole 
• 124413-27-0 3-amino-2-cyano-4'-methoxythiocinnamaldehyde 
• 124413-52-1 3-amino-2-cyano-4'-methoxycinnamaldehyde 
• 94775-46-9 3,5-Dicyano-2-(4-methoxyphenyl)-6-(3-tolyl)-4-thiopyridone 
• 84302-58-9 4-(4-Methoxy-phenyl)-2-(4-nitro-phenyl)-thiazole-5-carbonitrile 
• 84302-62-5 2-(4-Dimethylamino-phenyl)-4-(4-methoxy-phenyl)-thiazole-5-carbonitrile 

Relevant articles and documents

Acid-promoted rapid solvent-free access to substituted 1,4-dihydropyridines from β-ketothioamides

β-Ketothioamides (KTAs) have been used as building blocks with aldehydes and β-enaminonitriles for synthesis of 1,4-dihydropyridines in the presence of AcOH under solvent-free conditions within 5 min. This new strategy exhibits remarkable features such as high chemoselectivity, mild reaction conditions, easily available substrates, and good yields.

Rhodium-catalyzed asymmetric hydrogenation of β-acetylamino acrylonitriles

The rhodium-catalyzed asymmetric hydrogenation of β-acetylamino acrylonitriles was investigated by using monophosphine and bisphosphine ligands. It was found that an Rh-QuinoxP complex exhibited high enantioselectivities for β-aryl substituted β-acetylamino acrylonitriles and the Rh-JosiPhos CyPF-t-Bu complex was proven to be effective for the hydrogenation of tetrasubstituted olefins from cyclic β-acetylamino acrylonitriles.

Addition of acetonitrile anions to unsaturated systems under ultrasonically dispersed potassium system

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